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DOI: 10.1055/s-0039-1681225
YIELD OF MALIGNANT LYMPH NODE DETECTION BY EUS AND FNA IN RESTAGING AFTER NEOADJUVANT CHEMORADIOTHERAPY FOR OESOPHAGEAL CANCER
Publication History
Publication Date:
18 March 2019 (online)
Aims:
Despite the known decreased accuracy, endoscopic ultrasonography (EUS) and fine-needle aspiration (FNA) are believed to be potential tools for detection of residual disease after neoadjuvant chemoradiotherapy (nCRT) for oesophageal cancer. This study aimed to investigate the yield of EUS and FNA for detection of malignant lymph nodes after nCRT.
Methods:
EUS and FNA were performed 12 weeks after completion of nCRT. Suspect lymph nodes were defined as round, hypo-echogenic, and with a size of ≥5 millimetres. Lymph nodes that were considered suspect but did not meet aforementioned criteria were recorded separately. To guide targeting of suspect lymph nodes, F18-FDG PET-CT was performed beforehand. Endoscopic nodal staging by EUS (uN) was compared to the histopathological examination of the resection specimen (ypN). Primary outcome of this study was the proportion of patients with malignant lymph nodes (ypN+) that was identified by EUS (uN+).
Results:
100 consecutive patients were included in this analysis. Tumour was passable in all patients. Twenty-one patients had ypN+ residual disease of which 11 were identified by EUS (sensitivity 52%). Subsequently, 62 of 79 ypN- patients were classified accordingly by EUS (specificity 78%). More than half of patients (n = 6, 55%) in whom suspect lymph nodes did not meet predefined criteria had ypN+ residual disease. Missed malignant lymph nodes were located at the coeliac trunk, the lesser curvature, and at the paraoesophageal stations. Sensitivity and specificity of FNA were 75% (3/4) and 100% (11/11), respectively. FNA outcome was uncertain in 8 patients. A positive aspirate was collected in one FDG-avid lymph node that was deemed benign by EUS.
Conclusions:
Only half of patients with ypN+ residual disease was identified by EUS after nCRT. For this reason and the absence of false-positive findings by FNA, all lymph nodes detected after nCRT should be sampled when aiming to detect residual disease.